*Manufacturing Documentation Support* role plays a key part in ensuring that all manufacturing documentation for medical devices is properly created, maintained, and compliant with regulatory standards.
Responsibilities:
* Ensure that all documents are up to date, accurate, and in compliance with relevant regulatory standards.
* Assist in the creation of documents for product specifications, protocols, and history files.
* Support the compliance of manufacturing documentation with regulatory requirements and internal quality standards.
* Coordinate with the Quality Assurance (QA) team to ensure the manufacturing processes and documentation adhere to industry regulations and company policies.
* Assist in internal audits and document reviews to ensure compliance with regulations.
Requirements
* Associate's degree or higher in a relevant field (e.g., Manufacturing, Engineering, Sciences, Business Administration, etc.).
* 2-4 years of experience in a manufacturing or quality assurance role in the medical device industry, with a focus on documentation or regulatory compliance.
* Bilingual (English & Spanish, written and spoken)
Job Types: Full-time, Contract
Schedule:
* 4 hour shift
Work Location: In person
